WS2C is a putative gene associated with Waardenburg syndrome type 2. It has not yet been isolated from its locus of chromosome 8p23 since it was first...
2 KB (155 words) - 00:11, 12 October 2020
chromosome 8 in the locus of 8p23. The gene has been provisionally termed WS2C. Type 2D is caused by an autosomal recessive mutation in both copies of the...
48 KB (5,759 words) - 18:57, 13 August 2024
Willebrand disease VWF dominant 1:10,000 Waardenburg syndrome PAX3, MITF, WS2B, WS2C, SNAI2, EDNRB, EDN3, SOX10 dominant 1:42,000 Warkany syndrome 2 8 trisomy...
42 KB (983 words) - 10:34, 21 August 2024